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Peer-reviewed veterinary case report

Best double-spin method to make platelet-rich plasma from dog blood

By Shin, Hyeok-Soo et al.·Published in BMC veterinary research·2017·College of Veterinary Medicine and Institute of Veterinary Science, South Korea·View original on PubMed

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Original publication title: Optimisation of a double-centrifugation method for preparation of canine platelet-rich plasma.

Species:
dog

Plain-English summary

A study found that using a specific double-centrifugation method can effectively prepare platelet-rich plasma (PRP) from dogs' blood, which is useful for healing and regenerative treatments. By first spinning the blood at 1000 g for 5 minutes and then at 1500 g for 15 minutes, the researchers achieved an 80% recovery of platelets and increased their concentration six-fold. This method also resulted in higher levels of a growth factor called PDGF-BB, which can aid in healing. This technique can be easily performed in veterinary clinics without needing expensive equipment.

People also search for: dog platelet-rich plasma treatment · how is PRP made for dogs · benefits of PRP for dog injuries

Abstract

BACKGROUND: Platelet-rich plasma (PRP) has been expected for regenerative medicine because of its growth factors. However, there is considerable variability in the recovery and yield of platelets and the concentration of growth factors in PRP preparations. The aim of this study was to identify optimal relative centrifugal force and spin time for the preparation of PRP from canine blood using a double-centrifugation tube method. METHODS: Whole blood samples were collected in citrate blood collection tubes from 12 healthy beagles. For the first centrifugation step, 10 different run conditions were compared to determine which condition produced optimal recovery of platelets. Once the optimal condition was identified, platelet-containing plasma prepared using that condition was subjected to a second centrifugation to pellet platelets. For the second centrifugation, 12 different run conditions were compared to identify the centrifugal force and spin time to produce maximal pellet recovery and concentration increase. Growth factor levels were estimated by using ELISA to measure platelet-derived growth factor-BB (PDGF-BB) concentrations in optimised CaCl-activated platelet fractions. RESULTS: The highest platelet recovery rate and yield were obtained by first centrifuging whole blood at 1000 g for 5 min and then centrifuging the recovered platelet-enriched plasma at 1500 g for 15 min. This protocol recovered 80% of platelets from whole blood and increased platelet concentration six-fold and produced the highest concentration of PDGF-BB in activated fractions. CONCLUSIONS: We have described an optimised double-centrifugation tube method for the preparation of PRP from canine blood. This optimised method does not require particularly expensive equipment or high technical ability and can readily be carried out in a veterinary clinical setting.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/28651609/